KNEE PAIN RELIEF PATCH WORMWOOD KNEE PATCH patch

Knee Pain Relief Patch Wormwood Knee Patch by

Drug Labeling and Warnings

Knee Pain Relief Patch Wormwood Knee Patch by is a Otc medication manufactured, distributed, or labeled by Guangzhou Baishili Trading Co., Ltd, Quanzhou Kuangmei Trade Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Health care function

Relieve neck, shoulder, waist, leg pain and promote health.

Usage

Opened the package back lining paper torn off，clean your skin where the discomfort,aim at the knee or discomfort parts were applied，the corresponding around six to eight hours per post.

Matters needing attention

1. The skin lesions were banned, allergic to wormwood careful.

2. During the period of a few people use local have tickling feeling or a red rash,does not afect theuse disappeared gradually after stopping.
3. The use of skin burns is a normal phenomenon.

Unsuitable people

Pregnant women, those allergic to wormwood are prohibited.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Apply one piece at a time, and each piece should be applied for 8 hours

INACTIVE INGREDIENT SECTION

MENTHOL 55%

DOSAGE & ADMINISTRATION

CAMPHOR 40%

BORNEOL 5%

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KNEE PAIN RELIEF PATCH WORMWOOD KNEE PATCH 
knee pain relief patch wormwood knee patch patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84727-022
Route of Administration	CONJUNCTIVAL, BUCCAL, CUTANEOUS, DENTAL, ELECTRO-OSMOSIS, AURICULAR (OTIC)

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	0.4 g  in 0.4 g
BORNEOL (UNII: M89NIB437X) (BORNEOL - UNII:M89NIB437X)	BORNEOL	0.4 g  in 0.4 g

Inactive Ingredients
Ingredient Name	Strength
MENTHOL (UNII: L7T10EIP3A)	0.4 g  in 0.4 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84727-022-02	36 in 1 PATCH	10/02/2024
1	NDC: 84727-022-01	36 g in 1 BOX; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	10/02/2024

Labeler - Guangzhou Baishili Trading Co., Ltd (709042161)

Registrant - Quanzhou Kuangmei Trade Co., Ltd. (841696421)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Baishili Trading Co., Ltd		709042161	manufacture(84727-022)